Cp*--ruthenium-nickel-based H2-evolving electrocatalysts as bio-inspired models of NiFe hydrogenases

European Journal of Inorganic Chemistry

Volumn , Issue 7, 2011, Pages 1094-1099

  Canaguier, Sigolène ^a   Fontecave, Marc ^a,b   Artero, Vincent ^a  

^a UNIV GRENOBLE ALPES   (France)

^b l'alimentation et l'Environnement   (France)

Author keywords

Biomimetic synthesis; Electrocatalysis; Enzyme models; Hydrogen; Metalloenzyme models; Nickel; Ruthenium

Indexed keywords

BINARY ALLOYS; BIOMIMETICS; ELECTROCATALYSIS; ELECTROCATALYSTS; IRON ALLOYS; NICKEL COMPOUNDS; RUTHENIUM COMPOUNDS; SYNTHESIS (CHEMICAL);

BIOINSPIRED MODELS; BIOMIMETIC SYNTHESIS; DINUCLEAR; ENZYME MODELS; METAL CENTRES; METALLOENZYME MODEL; METALLOENZYMES; PENTAMETHYLCYCLOPENTADIENYL; RUTHENIUM COMPLEXES; [NIFE]-HYDROGENASE;

HYDROGEN;

EID: 79951862386     PISSN: 14341948     EISSN: 10990682     Source Type: Journal    
DOI: 10.1002/ejic.201000944     Document Type: Article

References (20)

1. J. C. Fontecilla-Camps, A. Volbeda, C. Cavazza, Y. Nicolet, Chem. Rev. 2007, 107, 4273-4303.
2. A. K. Jones, E. Sillery, S. P. J. Albracht, F. A. Armstrong, Chem. Commun. 2002, 866-867.
3. S. Canaguier, V. Artero, M. Fontecave, Dalton Trans. 2008, 315-325.
4. C. Tard, C. J. Pickett, Chem. Rev. 2009, 109, 2245-2274.
5. B. E. Barton, C. M. Whaley, T. B. Rauchfuss, D. L. Gray, J. Am. Chem. Soc. 2009, 131, 6942-6943.
6. S. Canaguier, M. Field, Y. Oudart, J. Pécaut, M. Fontecave, V. Artero, Chem. Commun. 2010, 46, 5876-5878.
7. S. Ogo, R. Kabe, K. Uehara, B. Kure, T. Nishimura, S. C. Menon, R. Harada, S. Fukuzumi, Y. Higuchi, T. Ohhara, T. Tamada, R. Kuroki, Science 2007, 316, 585-587.
8. B. Kure, T. Matsumoto, K. Ichikawa, S. Fukuzumi, Y. Higuchi, T. Yagi, S. Ogo, Dalton Trans. 2008, 4747-4755.
9. T. Matsumoto, B. Kure, S. Ogo, Chem. Lett. 2008, 37, 970-971.
10. Y. Oudart, V. Artero, J. Pécaut, C. Lebrun, M. Fontecave, Eur. J. Inorg. Chem. 2007, 2613-2626.
11. S. Canaguier, L. Vaccaro, V. Artero, R. Ostermann, J. Pécaut, M. Field, M. Fontecave, Chem. Eur. J. 2009, 15, 9350-9365.
12. L. Vaccaro, V. Artero, S. Canaguier, M. Fontecave, J. M. Field, Dalton Trans. 2010, 39, 3043-3049.
13. Y. Oudart, V. Artero, J. Pécaut, M. Fontecave, Inorg. Chem. 2006, 45, 4334-4336.
14. J. A. W. Verhagen, D. D. Ellis, M. Lutz, A. L. Spek, E. Bouwman, J. Chem. Soc., Dalton Trans. 2002, 1275-1280.
15. M. A. Reynolds, T. B. Rauchfuss, S. R. Wilson, Organometallics 2003, 22, 1619-1625.
16. Comparison between the CH3CN and DMSO adducts is fully licit here because these ligands are likely eliminated from the Ru coordination sphere during the first reductive event.
17. R. M. Kellett, T. G. Spiro, Inorg. Chem. 1985, 24, 2373-2377.
18. X. Hu, B. S. Brunschwig, J. C. Peters, J. Am. Chem. Soc. 2007, 129, 8988-8998.
19. H. M. Koepp, H. Wedt, H. Strehlow, Z. Elektrochem. 1960, 64, 483.
20. M. Razavet, V. Artero, M. Fontecave, Inorg. Chem. 2005, 44, 4786-4795.